636 Management jobs in Somersworth
Senior Manager - Tax
Job Viewed
Job Description
14 hours ago Be among the first 25 applicants Get AI-powered advice on this job and more exclusive features. Direct message the job poster from KBW Financial Staffing & Recruiting Public Accounting Recruitment Specialist | Aligning Public Accounting Talent with the Right Opportunities Ready to shape the future of a thriving boutique tax and advisory firm? Join our client's tenured team in the Tri-City area of New Hampshire as a Tax Manager , where you’ll drive tax strategy, engage with diverse clients, and grow toward a partner role. Reporting to a seasoned partner, you’ll thrive in a collaborative onsite role (5 days/week), leveraging your ambition to unlock significant financial upside. Salary : Competitive, experience-aligned salary starting at $160,000 (DOE) Location : Onsite role based in Tri-City, NH (5 days/week in-office). Note : The company is unable to sponsor candidates at this time. Why Join Us? Partner Track: Clear path to ownership/partner role with mentorship from experienced leaders. Dynamic Growth: Join a firm with aggressive expansion, fueled by new business and future retirements. Diverse Opportunities: Specialize in business or personal tax. Collaborative Culture: Thrive in a small, family-like firm. Competitive Rewards: Competitive salary starting at $30,000+, plus 100% paid health benefits for you and your family. Work-Life Balance: Enjoy early-release Fridays and a balanced workload outside peak tax season. What You’ll Do Lead tax planning and compliance for a diverse client portfolio, including businesses and high-net-worth individuals. Engage directly with clients, providing trusted advice on tax strategies and multi-state filings. Prepare and review complex tax returns, ensuring accuracy and regulatory compliance. Mentor junior staff, fostering a collaborative environment and sharing expertise. Drive process improvements to enhance tax and advisory workflows across the firm. What We’re Looking For Experience: 8+ years in public accounting, with at least some tax experience; diverse industry exposure a plus. Education: Bachelor’s degree in Accounting or related field; advanced degree a plus. Certifications: CPA required for partner track Skills: Exceptional communication and client-facing skills to build trust without needing oversight. Mindset: Ambitious, eager to grow into an owner/partner, and thrives in a collaborative, fast-paced setting. Technical Skills: Proficiency in tax software and Excel; experience with multi-state filings preferred. Location: Local to the Nashua/Boston area for onsite work (5 days/week). Preferences: Interest in business valuation, litigation support, or trust/estate services a plus. Ready to Build a Legacy in Tax Leadership? Join a boutique advisory firm where your ambition will drive success and partnership! Submit your resume to Alden Flagg at today. Don’t miss this chance to thrive in a high-growth, client-focused role! KBW789 Seniority level Seniority level Mid-Senior level Employment type Employment type Full-time Job function Job function Accounting/Auditing and Finance Industries Staffing and Recruiting Referrals increase your chances of interviewing at KBW Financial Staffing & Recruiting by 2x Get notified about new Senior Tax Manager jobs in Somersworth, NH . Portsmouth, NH $70,000. 0- 78,000.00 2 months ago Somersworth, NH 65,000.00- 75,000.00 5 days ago Portsmouth, NH 62,000.00- 85,000.00 2 weeks ago Rochester, NH 200,000.00- 250,000.00 5 days ago Portsmouth, NH 70,000.00- 95,000.00 2 weeks ago Rochester, NH 85,000.00- 120,000.00 1 hour ago Rochester, NH 95,000.00- 120,000.00 5 days ago Region Advancement Director - Boston, MA, Providence, RI, Southern New Hampshire,Southern Maine Portsmouth, NH 107,000.00- 117,000.00 1 week ago Portsmouth, NH 50,000.00- 80,000.00 1 week ago We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr
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Travel Nurse RN - Case Management - $2,660 per week
Posted today
Job Viewed
Job Description
HealthTrust Workforce Solutions HCA is seeking a travel nurse RN Case Management for a travel nursing job in Portsmouth, New Hampshire.
Job Description & Requirements- Specialty: Case Management
- Discipline: RN
- Start Date: ASAP
- Duration: 13 weeks
- 40 hours per week
- Shift: 8 hours, days
- Employment Type: Travel
899562
About HealthTrust Workforce Solutions HCAAt HealthTrust Workforce Solutions, healthcare is not just about the four walls of a facility but about the people who provide and receive care. Our focus is on empowering healthcare professionals to deliver exceptional patient experiences by providing them with the necessary skills, tools, and support. We partner with healthcare facilities nationwide to ensure that the right professionals are in the right roles. We prioritize our clinicians by giving them a voice and access to opportunities to fulfill their mission of improving lives by providing quality patient care.
We are committed to our core values of Trust, Innovation, Adaptability, Courage, and Accountability. We are dedicated to positively impacting the healthcare industry by providing first-priority access to more than 200,000 jobs nationwide to our healthcare professionals. Join us and be part of the HealthTrust family, where you can make a difference every day.
We embrace our changing environment, and we maintain a culture that has a rich tradition of transforming itself to meet the challenges of the future.
MISSION STATEMENT
While putting great people in the right roles is essential, our mission is far greater. We want our clinicians to be part of the HealthTrust family, where healthcare professionals have a voice and are empowered with the right tools and opportunities to fulfill their personal mission of improving lives. Plus, as a preferred partner to thousands of top-performing hospitals, we provide our healthcare professionals with first-priority access to more than 200,000 jobs nationwide.
Benefits- Dental benefits
- Vision benefits
- Referral bonus
- Continuing Education
- Life insurance
RN Clinical Manager
Posted today
Job Viewed
Job Description
At Caretenders, a part of LHC Group, we embrace a culture of caring, belonging, and trust and enjoy the meaningful connections that come from it: for the whole patient, their families, each other, and the communities we serve—it truly is all about helping people. You can find a home for your career here.
As a Patient Care Manager, you can expect:
* opportunities to get closer to patients and provide quality support to your patient-facing teams
* to be valued and respected by patients and their families
* a sense of security, incredible team support, and flexibility for true work-life balance
* leadership development opportunities
Our Patient Care Manager role might be a great opportunity if you believe in putting the patient at the center of everything. Apply today!
The Home Health Patient Care Manager is responsible for the supervision and coordination of clinical services and provides and directs provisions of nursing care to patients in their homes as prescribed by the physician and in compliance with applicable laws, regulations, and agency policies.
* Provides clinical services within the scope of practice, as defined by the state laws governing the practice of nursing, in accordance with the plan of care, and in coordination with other members of the health care team.
* Receives referrals, ensures appropriate clinician assignments, evaluate patient orders, and plot start of care visits.
* Coordinates determination of patient home health benefits, medical necessity, and ongoing insurance approvals.
* Ensures patient needs are continually assessed and care rendered is individualized to patient needs, appropriate and reasonable, meets home health eligibility criteria, and is in accordance with physician orders.
* Reviews assessments and plans of care daily, per assigned workflow, and consults clinicians with recommendations, as appropriate.
Education & Experience
* Current RN licensure in state of practice
* Current CPR certification required
* Current Driver's License, vehicle insurance, and access to a dependable vehicle or public transportation
By applying, you consent to your information being transmitted by Get It to the Employer, as data controller, through the Employer's data processor SonicJobs.
See LHC Group Privacy Policy at and SonicJobs Privacy Policy at and Terms of Use at
GMP Manufacturing Manager
Posted today
Job Viewed
Job Description
The actual location of this job is in Portsmouth, NH. Relocation assistance is available for eligible candidates and their families, if needed.
Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.
Join a global team of over 18,000 people making a meaningful difference from day one. As a GMP Manufacturing Supervisor at our Portsmouth site you will coordinate and support production activities for Cell and Gene processes.
Find out more about what a life at Lonza in Portsmouth, NH could look like for you by watching this short video.
What you’ll get:
An agile career and dynamic working culture.
An inclusive and ethical workplace.
Compensation programs that recognize high performance.
Medical, dental and vision insurance.
The full list of our global benefits can be also found on .
What you’ll do:
Coordinate and support the execution of Cell and Gene production activities, ensuring compliance with ET and site quality systems.
Lead and develop the manufacturing team to meet business needs and career goals.
Support the timely and complete delivery of clinical and commercial materials.
Coordinate various strategies, including EHS, Training, Gowning, Material, Visual Inspection, APS, Cleaning, Scheduling, Financial Management and EM.
Maintain manufacturing areas to the highest cleanliness and 6S standards.
Support technology transfer activities and ensure timely goal achievement.
Establish methods and procedures for attaining specific goals.
What we’re looking for:
BS degree preferred significant experience may be considered in lieu of degree.
Minimum 5 years related experience with a degree or 8 years without.
Proven experience in biological GMP manufacturing operations.
Strong leadership and team development skills.
Ability to coordinate complex projects and ensure timely delivery.
Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.
Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.
GMP Production Manager
Posted today
Job Viewed
Job Description
Open to relocation
Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.
Join a global team of over 18,000 people making a meaningful difference from day one. As a GMP Manufacturing Supervisor at our Portsmouth site you will coordinate and support production activities for Cell and Gene processes.
Find out more about what a life at Lonza in Portsmouth, NH could look like for you by watching this short video.
What you’ll get:
An agile career and dynamic working culture.
A highly collaborative work environment that values best practice sharing.
An inclusive and ethical workplace.
Compensation programs that recognize high performance.
What you’ll do:
Coordinate and support production activities for Cell and Gene processes.
Understand and communicate module-specific processing needs to manufacturing associates.
Facilitate setup and execution of manufacturing procedures following ET and site quality systems.
Develop the manufacturing team to meet business and personal goals.
Support on-time delivery of clinical and commercial material.
Support and ensure execution of EHS, Training, Gowning, Material, Visual Inspection, APS, Cleaning, Scheduling, Financial Management, and EM strategies.
Perform other duties as assigned.
BS Preferred, additional experience in lieu of degree considered.
Minimum 5 years related experience with degree, minimum 8 years without degree.
Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.
Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.
GMP Production Manager
Posted today
Job Viewed
Job Description
The actual location of this job is in Portsmouth, NH. Relocation assistance is available for eligible candidates and their families, if needed.
Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.
Join a global team of over 18,000 people making a meaningful difference from day one. As a GMP Manufacturing Supervisor at our Portsmouth site you will coordinate and support production activities for Cell and Gene processes.
Find out more about what a life at Lonza in Portsmouth, NH could look like for you by watching this short video.
What you’ll get:
An agile career and dynamic working culture.
An inclusive and ethical workplace.
Compensation programs that recognize high performance.
Medical, dental and vision insurance.
The full list of our global benefits can be also found on .
What you’ll do:
Coordinate and support the execution of Cell and Gene production activities, ensuring compliance with ET and site quality systems.
Lead and develop the manufacturing team to meet business needs and career goals.
Support the timely and complete delivery of clinical and commercial materials.
Coordinate various strategies, including EHS, Training, Gowning, Material, Visual Inspection, APS, Cleaning, Scheduling, Financial Management and EM.
Maintain manufacturing areas to the highest cleanliness and 6S standards.
Support technology transfer activities and ensure timely goal achievement.
Establish methods and procedures for attaining specific goals.
What we’re looking for:
BS degree preferred significant experience may be considered in lieu of degree.
Minimum 5 years related experience with a degree or 8 years without.
Proven experience in biological GMP manufacturing operations.
Strong leadership and team development skills.
Ability to coordinate complex projects and ensure timely delivery.
Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.
Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.
GMP Production Manager
Posted today
Job Viewed
Job Description
The actual location of this job is in Portsmouth, NH. Relocation assistance is available for eligible candidates and their families, if needed.
Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.
Join a global team of over 18,000 people making a meaningful difference from day one. As a GMP Manufacturing Supervisor at our Portsmouth site you will coordinate and support production activities for Cell and Gene processes.
Find out more about what a life at Lonza in Portsmouth, NH could look like for you by watching this short video.
What you’ll get:
An agile career and dynamic working culture.
An inclusive and ethical workplace.
Compensation programs that recognize high performance.
Medical, dental and vision insurance.
The full list of our global benefits can be also found on .
What you’ll do:
Coordinate and support the execution of Cell and Gene production activities, ensuring compliance with ET and site quality systems.
Lead and develop the manufacturing team to meet business needs and career goals.
Support the timely and complete delivery of clinical and commercial materials.
Coordinate various strategies, including EHS, Training, Gowning, Material, Visual Inspection, APS, Cleaning, Scheduling, Financial Management and EM.
Maintain manufacturing areas to the highest cleanliness and 6S standards.
Support technology transfer activities and ensure timely goal achievement.
Establish methods and procedures for attaining specific goals.
What we’re looking for:
BS degree preferred significant experience may be considered in lieu of degree.
Minimum 5 years related experience with a degree or 8 years without.
Proven experience in biological GMP manufacturing operations.
Strong leadership and team development skills.
Ability to coordinate complex projects and ensure timely delivery.
Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.
Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.
GMP Production Manager
Posted today
Job Viewed
Job Description
Open to relocation
Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.
Join a global team of over 18,000 people making a meaningful difference from day one. As a GMP Manufacturing Supervisor at our Portsmouth site you will coordinate and support production activities for Cell and Gene processes.
Find out more about what a life at Lonza in Portsmouth, NH could look like for you by watching this short video.
What you’ll get:
An agile career and dynamic working culture.
A highly collaborative work environment that values best practice sharing.
An inclusive and ethical workplace.
Compensation programs that recognize high performance.
What you’ll do:
Coordinate and support production activities for Cell and Gene processes.
Understand and communicate module-specific processing needs to manufacturing associates.
Facilitate setup and execution of manufacturing procedures following ET and site quality systems.
Develop the manufacturing team to meet business and personal goals.
Support on-time delivery of clinical and commercial material.
Support and ensure execution of EHS, Training, Gowning, Material, Visual Inspection, APS, Cleaning, Scheduling, Financial Management, and EM strategies.
Perform other duties as assigned.
BS Preferred, additional experience in lieu of degree considered.
Minimum 5 years related experience with degree, minimum 8 years without degree.
Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.
Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.
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GMP Manufacturing Manager
Posted today
Job Viewed
Job Description
Open to relocation
Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.
Join a global team of over 18,000 people making a meaningful difference from day one. As a GMP Manufacturing Supervisor at our Portsmouth site you will coordinate and support production activities for Cell and Gene processes.
Find out more about what a life at Lonza in Portsmouth, NH could look like for you by watching this short video.
What you’ll get:
An agile career and dynamic working culture.
A highly collaborative work environment that values best practice sharing.
An inclusive and ethical workplace.
Compensation programs that recognize high performance.
What you’ll do:
Coordinate and support production activities for Cell and Gene processes.
Understand and communicate module-specific processing needs to manufacturing associates.
Facilitate setup and execution of manufacturing procedures following ET and site quality systems.
Develop the manufacturing team to meet business and personal goals.
Support on-time delivery of clinical and commercial material.
Support and ensure execution of EHS, Training, Gowning, Material, Visual Inspection, APS, Cleaning, Scheduling, Financial Management, and EM strategies.
Perform other duties as assigned.
BS Preferred, additional experience in lieu of degree considered.
Minimum 5 years related experience with degree, minimum 8 years without degree.
Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.
Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.
GMP Manufacturing Manager
Posted today
Job Viewed
Job Description
Open to relocation
Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.
Join a global team of over 18,000 people making a meaningful difference from day one. As a GMP Manufacturing Supervisor at our Portsmouth site you will coordinate and support production activities for Cell and Gene processes.
Find out more about what a life at Lonza in Portsmouth, NH could look like for you by watching this short video.
What you’ll get:
An agile career and dynamic working culture.
A highly collaborative work environment that values best practice sharing.
An inclusive and ethical workplace.
Compensation programs that recognize high performance.
What you’ll do:
Coordinate and support production activities for Cell and Gene processes.
Understand and communicate module-specific processing needs to manufacturing associates.
Facilitate setup and execution of manufacturing procedures following ET and site quality systems.
Develop the manufacturing team to meet business and personal goals.
Support on-time delivery of clinical and commercial material.
Support and ensure execution of EHS, Training, Gowning, Material, Visual Inspection, APS, Cleaning, Scheduling, Financial Management, and EM strategies.
Perform other duties as assigned.
BS Preferred, additional experience in lieu of degree considered.
Minimum 5 years related experience with degree, minimum 8 years without degree.
Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.
Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.
GMP Manufacturing Manager
Posted today
Job Viewed
Job Description
The actual location of this job is in Portsmouth, NH. Relocation assistance is available for eligible candidates and their families, if needed.
Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.
Join a global team of over 18,000 people making a meaningful difference from day one. As a GMP Manufacturing Supervisor at our Portsmouth site you will coordinate and support production activities for Cell and Gene processes.
Find out more about what a life at Lonza in Portsmouth, NH could look like for you by watching this short video.
What you’ll get:
An agile career and dynamic working culture.
An inclusive and ethical workplace.
Compensation programs that recognize high performance.
Medical, dental and vision insurance.
The full list of our global benefits can be also found on .
What you’ll do:
Coordinate and support the execution of Cell and Gene production activities, ensuring compliance with ET and site quality systems.
Lead and develop the manufacturing team to meet business needs and career goals.
Support the timely and complete delivery of clinical and commercial materials.
Coordinate various strategies, including EHS, Training, Gowning, Material, Visual Inspection, APS, Cleaning, Scheduling, Financial Management and EM.
Maintain manufacturing areas to the highest cleanliness and 6S standards.
Support technology transfer activities and ensure timely goal achievement.
Establish methods and procedures for attaining specific goals.
What we’re looking for:
BS degree preferred significant experience may be considered in lieu of degree.
Minimum 5 years related experience with a degree or 8 years without.
Proven experience in biological GMP manufacturing operations.
Strong leadership and team development skills.
Ability to coordinate complex projects and ensure timely delivery.
Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.
Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.